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香叶基丙酮和釉原蛋白联合应用促进人牙周膜细胞血管生成和伤口愈合。

Combined application of geranylgeranylacetone and amelogenin promotes angiogenesis and wound healing in human periodontal ligament cells.

机构信息

Division of Oral Rehabilitation, Department of Periodontology, Faculty of Dental Science, Kyushu University, Fukuoka, Japan.

Dental and Oral Medical Center, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

出版信息

J Cell Biochem. 2021 Jul;122(7):716-730. doi: 10.1002/jcb.29903. Epub 2021 Feb 2.

Abstract

Amelogenin directly binds to glucose-regulated protein 78 (Grp78). Cell migration activity is expected to increase when human periodontal ligament cells (hPDLCs) overexpressing Grp78 are treated with amelogenin. Geranylgeranylacetone (GGA) is a drug that induces the expression of heat shock protein and is routinely used to treat gastric ulcers. Here, we investigated the changes in the properties and behavior of hPDLCs in response to treatment with GGA and the synergistic effects of amelogenin stimulation in hPDLCs pretreated with GGA for the establishment of a novel periodontal tissue regenerative therapy. We observed that GGA treatment increased Grp78 protein expression in hPDLCs and enhanced cell migration. Microarray analysis demonstrated that increased Grp78 expression triggered the production of angiopoietin-like 4 and amphiregulin, which are involved in the enhancement of angiogenesis and subsequent wound healing via the activation of hypoxia-inducible factor 1α and peroxisome proliferator-activated receptors as well as the phosphorylation of cAMP response element-binding protein and protein kinase A. Moreover, the addition of recombinant murine amelogenin (rM180) further accelerated hPDLC migration and tube formation of human umbilical vein endothelial cells due to the upregulation of interleukin-8 (IL-8), monocyte chemotactic protein 1, and IL-6, which are also known as angiogenesis-inducing factors. These findings suggest that the application of GGA to gingival tissue and alveolar bone damaged by periodontal disease would facilitate the wound healing process by inducing periodontal ligament cells to migrate to the root surface and release cytokines involved in tissue repair. Additionally, supplementation with amelogenin synergistically enhanced the migratory capacity of these cells while actively promoting angiogenesis. Therefore, the combined application of GGA and amelogenin may establish a suitable environment for periodontal wound healing and further drive the development of novel therapeutics for periodontal tissue regeneration.

摘要

成釉蛋白直接与葡萄糖调节蛋白 78(Grp78)结合。当过表达 Grp78 的人牙周韧带细胞(hPDLCs)用成釉蛋白处理时,细胞迁移活性预计会增加。香叶基丙酮(GGA)是一种诱导热休克蛋白表达的药物,常用于治疗胃溃疡。在这里,我们研究了 GGA 处理对 hPDLCs 特性和行为的变化,以及 GGA 预处理对 hPDLCs 中釉原蛋白刺激的协同作用,以建立一种新的牙周组织再生治疗方法。我们观察到 GGA 处理增加了 hPDLCs 中 Grp78 蛋白的表达,并增强了细胞迁移。微阵列分析表明,Grp78 表达的增加触发了血管生成素样 4 和 Amphiregulin 的产生,这两种蛋白通过激活缺氧诱导因子 1α 和过氧化物酶体增殖物激活受体以及 cAMP 反应元件结合蛋白和蛋白激酶 A 的磷酸化,参与血管生成和随后的伤口愈合。此外,由于白细胞介素-8(IL-8)、单核细胞趋化蛋白 1 和 IL-6 的上调,重组鼠釉原蛋白(rM180)的添加进一步加速了 hPDLC 的迁移和人脐静脉内皮细胞的管形成,这些蛋白也被称为血管生成诱导因子。这些发现表明,将 GGA 应用于牙周病引起的牙龈组织和牙槽骨损伤,通过诱导牙周韧带细胞迁移到根表面并释放参与组织修复的细胞因子,将促进伤口愈合过程。此外,补充釉原蛋白协同增强了这些细胞的迁移能力,同时积极促进血管生成。因此,GGA 和釉原蛋白的联合应用可能为牙周伤口愈合创造合适的环境,并进一步推动牙周组织再生的新型治疗方法的发展。

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